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Eli Lilly CDR (CAD Hedged)

Eli Lilly CDR (CAD Hedged) logo
🇺🇸United States
Ownership
-
Employees
43K
Market Cap
$859.4B
Website
Introduction

Eli Lilly & Co. engages in the discovery, development, manufacture, and sale of pharmaceutical products. The firm's products consist of diabetes, oncology, immunology, neuroscience, and other products and therapies. The company was founded by Eli Lilly in May 1876 and is headquartered in Indianapolis, IN.

Clinical Trials

3.5k

Active:1479
Completed:1701

Trial Phases

6 Phases

Early Phase 1:1
Phase 1:1704
Phase 2:488
+3 more phases

Drug Approvals

91

SFDA:39
FDA:38
NMPA:13
+1 more agencies

Drug Approvals

Donanemab Injection

Product Name
记能达
Approval Number
国药准字SJ20240047
Approval Date
Dec 17, 2024
NMPA

Ixekizumab Injection

Product Name
拓咨
Approval Number
国药准字SJ20190034
Approval Date
Sep 10, 2024
NMPA

Duloxetine Hydrochloride Enteric Capsules

Product Name
欣百达
Approval Number
国药准字HJ20150284
Approval Date
Aug 6, 2024
NMPA

Duloxetine Hydrochloride Enteric Capsules

Product Name
欣百达
Approval Number
国药准字HJ20150285
Approval Date
Aug 6, 2024
NMPA

Duloxetine Hydrochloride Enteric Capsules

Product Name
欣百达
Approval Number
国药准字HJ20150287
Approval Date
Jun 27, 2024
NMPA

Duloxetine Hydrochloride Enteric Capsules

Product Name
欣百达
Approval Number
国药准字HJ20150286
Approval Date
Jun 27, 2024
NMPA

Ramucirumab Injection

Product Name
希冉择
Approval Number
国药准字SJ20220011
Approval Date
Mar 16, 2022
NMPA

Ramucirumab Injection

Product Name
希冉择
Approval Number
国药准字SJ20220012
Approval Date
Mar 16, 2022
NMPA

Ixekizumab Injection

Product Name
拓咨
Approval Number
S20190034
Approval Date
Aug 29, 2019
NMPA

Duloxetine Hydrochloride Enteric Capsules

Product Name
欣百达
Approval Number
H20150287
Approval Date
Jul 3, 2019
NMPA
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Clinical Trials

Distribution across different clinical trial phases (2990 trials with phase data)• Click on a phase to view related trials

Phase 1
1704 (57.0%)
Phase 3
602 (20.1%)
Phase 2
488 (16.3%)
Phase 4
175 (5.9%)
Not Applicable
19 (0.6%)
Early Phase 1
1 (0.0%)
phase_2_3
1 (0.0%)

A Study of LY3549492 in Healthy Weight Adult Participants

Not Applicable
Not yet recruiting
Conditions
Healthy
Interventions
Drug: Placebo
First Posted Date
2025-07-25
Last Posted Date
2025-07-25
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
220
Registration Number
NCT07085468
Locations
🇺🇸

Headlands Research - Scottsdale, Scottsdale, Arizona, United States

🇺🇸

Valley Clinical Trials, Inc., Northridge, California, United States

🇺🇸

Peninsula Research Associates, Rolling Hills Estates, California, United States

and more 16 locations

A Study of LY3549492 in Chinese Participants With Type 2 Diabetes Mellitus

Not Applicable
Not yet recruiting
Conditions
Type 2 Diabetes
Interventions
Drug: Placebo
First Posted Date
2025-07-18
Last Posted Date
2025-07-18
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
36
Registration Number
NCT07073170
Locations
🇨🇳

Peking University First Hospital, Dongcheng District, Beijing, China

🇨🇳

West China Hospital of Sichuan University, Chengdu, Sichuan, China

🇨🇳

Peking University People's Hospital, Beijing, China

A Study of Remternetug (LY3372993) in Healthy Participants

Not Applicable
Recruiting
Conditions
Healthy
Interventions
Drug: Remternetug (Test)
Drug: Remternetug (Reference)
First Posted Date
2025-07-09
Last Posted Date
2025-07-23
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
72
Registration Number
NCT07056309
Locations
🇺🇸

Fortrea Clinical Research Unit, Dallas, Texas, United States

🇺🇸

QPS Missouri, Springfield, Missouri, United States

A Study of LY4175408 in Participants With Advanced Cancer

Not Applicable
Not yet recruiting
Conditions
Neoplasm Metastasis
Triple Negative Breast Cancer
Carcinoma, Non-Small-Cell Lung
Small Cell Lung Carcinoma
Endometrial Neoplasms
Interventions
First Posted Date
2025-07-02
Last Posted Date
2025-07-23
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
240
Registration Number
NCT07046923
Locations
🇺🇸

The Ohio State University (OSU) Wexner Medical Center, Columbus, Ohio, United States

🇺🇸

START Mountain Region, West Valley City, Utah, United States

🇺🇸

Stanford Cancer Center, Stanford, California, United States

and more 20 locations

A Single- and Multiple-Ascending Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of LY4066708 in Healthy Participants

Not Applicable
Recruiting
Conditions
Healthy
Cancer
Interventions
Drug: LY4066708
Drug: Placebo
First Posted Date
2025-07-01
Last Posted Date
2025-07-23
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
104
Registration Number
NCT07046559
Locations
🇬🇧

Fortrea Clinical Research Unit, Holbeck, Leeds, Leeds, United Kingdom

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News

Adocia's Ultra-Rapid Insulin BioChaperone Lispro Meets Primary Endpoint in Phase 3 Trial for Type 2 Diabetes

BioChaperone Lispro (THDB0206) demonstrated non-inferior HbA1c reduction compared to Humalog in a Phase 3 trial of 1,040 Chinese adults with Type 2 diabetes.

Gate Bioscience Partners with Lilly in $856 Million Deal to Develop Novel Molecular Gate Therapeutics

Gate Bioscience announced a collaboration and license agreement with Eli Lilly to discover and develop molecular gate therapeutics, a new class of small molecule drugs that eliminate disease-causing proteins at their source.

Roche Explores Direct-to-Consumer Drug Sales Model to Reduce US Patient Costs

Roche is considering selling prescription medicines directly to US consumers to lower patient costs, following government pressure to reduce drug prices.

IXICO Secures Full Data Rights to Landmark Bio-Hermes-002 Alzheimer's Study Through Strategic GAP Partnership

IXICO has deepened its collaboration with the Global Alzheimer's Platform Foundation through an agreement securing full data usage rights to the Bio-Hermes-002 study, one of the most prominent global studies in Alzheimer's disease research.

Eli Lilly Advances LOXO-435 in Phase 1 FORAGER-1 Study for FGFR3-Altered Advanced Cancers

Eli Lilly's FORAGER-1 Phase 1 study is evaluating LOXO-435 (LY3866288) as both monotherapy and combination treatment for locally advanced or metastatic solid tumors with FGFR3 gene alterations.

Livzon's Dual-Target IL-17A/F Antibody LZM012 Outperforms Secukinumab in Phase III Psoriasis Trial

Livzon Pharmaceutical's LZM012, the first domestic dual-target IL-17A/F monoclonal antibody, achieved superior efficacy compared to Secukinumab in a Phase III trial for moderate to severe plaque psoriasis.

Omega Funds Closes Oversubscribed $647M Fund VIII to Accelerate Life Sciences Innovation

Omega Funds successfully closed its eighth fund with $647 million in capital commitments, exceeding its $600 million target despite challenging fundraising conditions.

Bristol Myers Squibb and Pfizer Launch Direct-to-Patient Eliquis Program with 40% Price Discount

Bristol Myers Squibb and Pfizer announced a new direct-to-patient purchasing option for Eliquis (apixaban) through their Eliquis 360 Support program, offering eligible patients a cash price more than 40% below the current $606 list price.

FDA Implements Major Workforce Reduction and Policy Changes Amid Regulatory Overhaul

Up to 3,500 FDA staffers received termination notices following a Supreme Court ruling that found the government's HHS overhaul to be lawful.

Hengrui and Kailera's Dual GLP-1/GIP Obesity Drug Achieves 18% Weight Loss in Phase 3 Trial

Hengrui Pharma and Kailera Therapeutics' dual-acting obesity drug HRS9531 demonstrated 18% weight loss in a Phase 3 trial in China, significantly outperforming placebo by 16%.

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